HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor
Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphoc...
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description | Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphocyte response to MSC and peripheral blood lymphocytes (PBL) from the MSC or third party donors was measured before and after infusion. In vitro primary and rechallenge lymphocyte responses of healthy individuals to MSC and to PBL from the MSC donor were similarly studied. HSCT recipients given MSC responded to third party allostimuli, but showed no response to infused MSC before and upto 6 months after infusion, whereas maintaining an alloresponse to the MSC donor. This indicates immune unresponsiveness restricted to MSC, as the HSCT recipient was not tolerized to the MSC donor. In vitro, we confirmed that MSC failed to prime responder lymphocytes to rechallenge with PBL from the MSC donor, and lymphocytes primed with MSC donor and rechallenged with MSC only showed weak responses at high stimulator-responder ratios. Although MSC up-regulated lymphocyte gene expression of CD25, IFN-gamma, FoxP3, CTLA-4, and IL-10, they failed in both unprimed and primed responders to induce CD25+ (activated) or CD57+ (effector) CD4+ or CD8+ T-lymphocyte subsets and only inconsistently induced FoxP3+ regulatory T-lymphocytes. These results show for the first time that infused MSC are only weakly immunogenic in humans and validate the clinical use of MSC from HLA-mismatched donors. |
doi_str_mv | 10.1097/CJI.0b013e3181ab1807 |
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John ; RINGDEN, Olle ; UZUNEL, Mehmet ; LINNIES, Helena ; DACKLAND, Asa-Lena ; CHRISTENSSON, Birger ; LE BLANC, Katarina</creator><creatorcontrib>SUNDIN, Mikael ; BARRETTE, A. John ; RINGDEN, Olle ; UZUNEL, Mehmet ; LINNIES, Helena ; DACKLAND, Asa-Lena ; CHRISTENSSON, Birger ; LE BLANC, Katarina</creatorcontrib><description>Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphocyte response to MSC and peripheral blood lymphocytes (PBL) from the MSC or third party donors was measured before and after infusion. In vitro primary and rechallenge lymphocyte responses of healthy individuals to MSC and to PBL from the MSC donor were similarly studied. HSCT recipients given MSC responded to third party allostimuli, but showed no response to infused MSC before and upto 6 months after infusion, whereas maintaining an alloresponse to the MSC donor. This indicates immune unresponsiveness restricted to MSC, as the HSCT recipient was not tolerized to the MSC donor. In vitro, we confirmed that MSC failed to prime responder lymphocytes to rechallenge with PBL from the MSC donor, and lymphocytes primed with MSC donor and rechallenged with MSC only showed weak responses at high stimulator-responder ratios. Although MSC up-regulated lymphocyte gene expression of CD25, IFN-gamma, FoxP3, CTLA-4, and IL-10, they failed in both unprimed and primed responders to induce CD25+ (activated) or CD57+ (effector) CD4+ or CD8+ T-lymphocyte subsets and only inconsistently induced FoxP3+ regulatory T-lymphocytes. These results show for the first time that infused MSC are only weakly immunogenic in humans and validate the clinical use of MSC from HLA-mismatched donors.</description><identifier>ISSN: 1524-9557</identifier><identifier>ISSN: 1053-8550</identifier><identifier>EISSN: 1537-4513</identifier><identifier>DOI: 10.1097/CJI.0b013e3181ab1807</identifier><identifier>PMID: 19561533</identifier><identifier>CODEN: JOIMF8</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott Williams & Wilkins</publisher><subject>Adolescent ; Adult ; Antineoplastic agents ; Biological and medical sciences ; CD8-Positive T-Lymphocytes - cytology ; CD8-Positive T-Lymphocytes - immunology ; CD8-Positive T-Lymphocytes - metabolism ; Child ; Female ; Flow Cytometry ; Gene Expression ; Graft vs Host Disease - immunology ; Hematopoietic Stem Cell Transplantation ; Histocompatibility Testing ; Humans ; Immunotherapy ; Infant ; Male ; Medical sciences ; Mesenchymal Stem Cell Transplantation ; Mesenchymal Stromal Cells - cytology ; Mesenchymal Stromal Cells - immunology ; Middle Aged ; Multipotent Stem Cells - cytology ; Multipotent Stem Cells - immunology ; Pharmacology. Drug treatments ; Reverse Transcriptase Polymerase Chain Reaction ; T-Lymphocytes - cytology ; T-Lymphocytes - immunology ; T-Lymphocytes - metabolism ; T-Lymphocytes, Regulatory - cytology ; T-Lymphocytes, Regulatory - immunology ; T-Lymphocytes, Regulatory - metabolism ; Tissue Donors ; Transplantation Tolerance - immunology ; Young Adult</subject><ispartof>Journal of immunotherapy, 2009-09, Vol.32 (7), p.755-764</ispartof><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c589t-bd2ade1f5aea7e3bcea2c325d31f0ff70e57615858017ec8a2d6e59c4be60e5c3</citedby><cites>FETCH-LOGICAL-c589t-bd2ade1f5aea7e3bcea2c325d31f0ff70e57615858017ec8a2d6e59c4be60e5c3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,550,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=21793517$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19561533$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:119129775$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>SUNDIN, Mikael</creatorcontrib><creatorcontrib>BARRETTE, A. John</creatorcontrib><creatorcontrib>RINGDEN, Olle</creatorcontrib><creatorcontrib>UZUNEL, Mehmet</creatorcontrib><creatorcontrib>LINNIES, Helena</creatorcontrib><creatorcontrib>DACKLAND, Asa-Lena</creatorcontrib><creatorcontrib>CHRISTENSSON, Birger</creatorcontrib><creatorcontrib>LE BLANC, Katarina</creatorcontrib><title>HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor</title><title>Journal of immunotherapy</title><addtitle>J Immunother</addtitle><description>Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphocyte response to MSC and peripheral blood lymphocytes (PBL) from the MSC or third party donors was measured before and after infusion. In vitro primary and rechallenge lymphocyte responses of healthy individuals to MSC and to PBL from the MSC donor were similarly studied. HSCT recipients given MSC responded to third party allostimuli, but showed no response to infused MSC before and upto 6 months after infusion, whereas maintaining an alloresponse to the MSC donor. This indicates immune unresponsiveness restricted to MSC, as the HSCT recipient was not tolerized to the MSC donor. In vitro, we confirmed that MSC failed to prime responder lymphocytes to rechallenge with PBL from the MSC donor, and lymphocytes primed with MSC donor and rechallenged with MSC only showed weak responses at high stimulator-responder ratios. Although MSC up-regulated lymphocyte gene expression of CD25, IFN-gamma, FoxP3, CTLA-4, and IL-10, they failed in both unprimed and primed responders to induce CD25+ (activated) or CD57+ (effector) CD4+ or CD8+ T-lymphocyte subsets and only inconsistently induced FoxP3+ regulatory T-lymphocytes. These results show for the first time that infused MSC are only weakly immunogenic in humans and validate the clinical use of MSC from HLA-mismatched donors.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Antineoplastic agents</subject><subject>Biological and medical sciences</subject><subject>CD8-Positive T-Lymphocytes - cytology</subject><subject>CD8-Positive T-Lymphocytes - immunology</subject><subject>CD8-Positive T-Lymphocytes - metabolism</subject><subject>Child</subject><subject>Female</subject><subject>Flow Cytometry</subject><subject>Gene Expression</subject><subject>Graft vs Host Disease - immunology</subject><subject>Hematopoietic Stem Cell Transplantation</subject><subject>Histocompatibility Testing</subject><subject>Humans</subject><subject>Immunotherapy</subject><subject>Infant</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mesenchymal Stem Cell Transplantation</subject><subject>Mesenchymal Stromal Cells - cytology</subject><subject>Mesenchymal Stromal Cells - immunology</subject><subject>Middle Aged</subject><subject>Multipotent Stem Cells - cytology</subject><subject>Multipotent Stem Cells - immunology</subject><subject>Pharmacology. Drug treatments</subject><subject>Reverse Transcriptase Polymerase Chain Reaction</subject><subject>T-Lymphocytes - cytology</subject><subject>T-Lymphocytes - immunology</subject><subject>T-Lymphocytes - metabolism</subject><subject>T-Lymphocytes, Regulatory - cytology</subject><subject>T-Lymphocytes, Regulatory - immunology</subject><subject>T-Lymphocytes, Regulatory - metabolism</subject><subject>Tissue Donors</subject><subject>Transplantation Tolerance - immunology</subject><subject>Young Adult</subject><issn>1524-9557</issn><issn>1053-8550</issn><issn>1537-4513</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>D8T</sourceid><recordid>eNqFklFv0zAQxy3ExErHN0AoL4ynbD47ziUvSCiDtVMR0lqeLce5sEAalzgd4tvj0GjQPcCTz_f_3V93umPsJfAL4DleFjfLC15ykCQhA1NCxvEJm4GSGCcK5NMxFkmcK4Wn7Ln3XzkXqUjEM3YKuUoDKGfserEuNtEt2WbXUDf4aGHuKVrvQqJubLRxLfWmsxQNLvq4LqJyP0SdG8bvcEe_U1euc_0ZO6lN6-nF9M7Z5w_vN8UiXn26XhbvVrFVWT7EZSVMRVArQwZJlpaMsFKoSkLN6xo5KQydZSrjgGQzI6qUVG6TktKgWTln8cHX_6DdvtS7vtma_qd2ptFT6luISIepRSoD__bAB2VLlQ0z9qY9KjtWuuZOf3H3WmCCiFkweDMZ9O77nvygt4231LamI7f3OoPQMHCO_yUxUakUuRzJ83-SKSoQIzpnyQG0vfO-p_qhceB6vAIdrkA_voJQ9urvof8UTWsPwOsJMN6ath5X3PgHTgDmUgHKX8dNu3M</recordid><startdate>20090901</startdate><enddate>20090901</enddate><creator>SUNDIN, Mikael</creator><creator>BARRETTE, A. John</creator><creator>RINGDEN, Olle</creator><creator>UZUNEL, Mehmet</creator><creator>LINNIES, Helena</creator><creator>DACKLAND, Asa-Lena</creator><creator>CHRISTENSSON, Birger</creator><creator>LE BLANC, Katarina</creator><general>Lippincott Williams & Wilkins</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>7T5</scope><scope>H94</scope><scope>5PM</scope><scope>ADTPV</scope><scope>AOWAS</scope><scope>D8T</scope><scope>ZZAVC</scope></search><sort><creationdate>20090901</creationdate><title>HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor</title><author>SUNDIN, Mikael ; BARRETTE, A. 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John</creatorcontrib><creatorcontrib>RINGDEN, Olle</creatorcontrib><creatorcontrib>UZUNEL, Mehmet</creatorcontrib><creatorcontrib>LINNIES, Helena</creatorcontrib><creatorcontrib>DACKLAND, Asa-Lena</creatorcontrib><creatorcontrib>CHRISTENSSON, Birger</creatorcontrib><creatorcontrib>LE BLANC, Katarina</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>Immunology Abstracts</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><collection>SwePub</collection><collection>SwePub Articles</collection><collection>SWEPUB Freely available online</collection><collection>SwePub Articles full text</collection><jtitle>Journal of immunotherapy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>SUNDIN, Mikael</au><au>BARRETTE, A. John</au><au>RINGDEN, Olle</au><au>UZUNEL, Mehmet</au><au>LINNIES, Helena</au><au>DACKLAND, Asa-Lena</au><au>CHRISTENSSON, Birger</au><au>LE BLANC, Katarina</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor</atitle><jtitle>Journal of immunotherapy</jtitle><addtitle>J Immunother</addtitle><date>2009-09-01</date><risdate>2009</risdate><volume>32</volume><issue>7</issue><spage>755</spage><epage>764</epage><pages>755-764</pages><issn>1524-9557</issn><issn>1053-8550</issn><eissn>1537-4513</eissn><coden>JOIMF8</coden><abstract>Multipotent mesenchymal stromal cells (MSC) are increasingly used to treat refractory graft-versus-host-disease and other complications after hematopoietic stem cell transplantation (HSCT). We evaluated immunogenicity of HLA-mismatched MSC infused posttransplant to HSCT recipients. Recipient lymphocyte response to MSC and peripheral blood lymphocytes (PBL) from the MSC or third party donors was measured before and after infusion. In vitro primary and rechallenge lymphocyte responses of healthy individuals to MSC and to PBL from the MSC donor were similarly studied. HSCT recipients given MSC responded to third party allostimuli, but showed no response to infused MSC before and upto 6 months after infusion, whereas maintaining an alloresponse to the MSC donor. This indicates immune unresponsiveness restricted to MSC, as the HSCT recipient was not tolerized to the MSC donor. In vitro, we confirmed that MSC failed to prime responder lymphocytes to rechallenge with PBL from the MSC donor, and lymphocytes primed with MSC donor and rechallenged with MSC only showed weak responses at high stimulator-responder ratios. Although MSC up-regulated lymphocyte gene expression of CD25, IFN-gamma, FoxP3, CTLA-4, and IL-10, they failed in both unprimed and primed responders to induce CD25+ (activated) or CD57+ (effector) CD4+ or CD8+ T-lymphocyte subsets and only inconsistently induced FoxP3+ regulatory T-lymphocytes. These results show for the first time that infused MSC are only weakly immunogenic in humans and validate the clinical use of MSC from HLA-mismatched donors.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott Williams & Wilkins</pub><pmid>19561533</pmid><doi>10.1097/CJI.0b013e3181ab1807</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adolescent Adult Antineoplastic agents Biological and medical sciences CD8-Positive T-Lymphocytes - cytology CD8-Positive T-Lymphocytes - immunology CD8-Positive T-Lymphocytes - metabolism Child Female Flow Cytometry Gene Expression Graft vs Host Disease - immunology Hematopoietic Stem Cell Transplantation Histocompatibility Testing Humans Immunotherapy Infant Male Medical sciences Mesenchymal Stem Cell Transplantation Mesenchymal Stromal Cells - cytology Mesenchymal Stromal Cells - immunology Middle Aged Multipotent Stem Cells - cytology Multipotent Stem Cells - immunology Pharmacology. Drug treatments Reverse Transcriptase Polymerase Chain Reaction T-Lymphocytes - cytology T-Lymphocytes - immunology T-Lymphocytes - metabolism T-Lymphocytes, Regulatory - cytology T-Lymphocytes, Regulatory - immunology T-Lymphocytes, Regulatory - metabolism Tissue Donors Transplantation Tolerance - immunology Young Adult |
title | HSCT Recipients Have Specific Tolerance to MSC but not to the MSC Donor |
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